EP1518564B1 - Hollow fiber blood-processing device - Google Patents

Hollow fiber blood-processing device Download PDF

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Publication number
EP1518564B1
EP1518564B1 EP04255856A EP04255856A EP1518564B1 EP 1518564 B1 EP1518564 B1 EP 1518564B1 EP 04255856 A EP04255856 A EP 04255856A EP 04255856 A EP04255856 A EP 04255856A EP 1518564 B1 EP1518564 B1 EP 1518564B1
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EP
European Patent Office
Prior art keywords
processing device
blood
hollow fibers
hollow fiber
container
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Expired - Lifetime
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EP04255856A
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German (de)
English (en)
French (fr)
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EP1518564A3 (en
EP1518564A2 (en
Inventor
Toshiaki c/o Nipro Corporation Masuda
Yuki c/o Nipro Corporation Hatakeyama
Takashi c/o Nipro Corporation Sunohara
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Nipro Corp
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Nipro Corp
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Priority claimed from JP2003330973A external-priority patent/JP4738728B2/ja
Priority claimed from JP2003330974A external-priority patent/JP4738729B2/ja
Application filed by Nipro Corp filed Critical Nipro Corp
Priority to PL04255856T priority Critical patent/PL1518564T3/pl
Publication of EP1518564A2 publication Critical patent/EP1518564A2/en
Publication of EP1518564A3 publication Critical patent/EP1518564A3/en
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/0005—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor for pharmaceuticals, biologicals or living parts
    • A61L2/0011—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor for pharmaceuticals, biologicals or living parts using physical methods
    • A61L2/0029—Radiation
    • A61L2/0035—Gamma radiation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
    • A61M1/16—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D65/00—Accessories or auxiliary operations, in general, for separation processes or apparatus using semi-permeable membranes
    • B01D65/02—Membrane cleaning or sterilisation ; Membrane regeneration
    • B01D65/022—Membrane sterilisation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
    • B01D67/0081—After-treatment of organic or inorganic membranes
    • B01D67/0097—Storing or preservation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
    • A61L2202/20—Targets to be treated
    • A61L2202/22—Blood or products thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2209/00—Ancillary equipment
    • A61M2209/06—Packaging for specific medical equipment
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2321/00—Details relating to membrane cleaning, regeneration, sterilization or to the prevention of fouling
    • B01D2321/34—Details relating to membrane cleaning, regeneration, sterilization or to the prevention of fouling by radiation
    • B01D2321/346—Details relating to membrane cleaning, regeneration, sterilization or to the prevention of fouling by radiation by gamma radiation

Definitions

  • the present invention relates to a hollow fiber blood-processing device used for blood processing such as hemodialysis, hemofiltration, hemodiafiltration, plasma fraction and plasmapheresis.
  • hollow fibers used as filters or semipermeable membranes in the blood-processing devices are generally damaged by radiation sterilization, resulting in increase of eluting materials or extractables from the hollow fibers.
  • the hollow fibers of polysulfone-based resins including hydrophilic polymer have a high tendency to be damaged by irradiation.
  • the extractables from the hollow fibers are measured by absorbance of a test solution for extraction, of which measuring procedures and criterion measure are defined in approval standards for artificial kidneys.
  • a test solution for extraction is prepared by placing 1.5g of dry hollow fibers cut to a length of 2 cm and 150 mL of distilled water for injection in a glass container that meets alkali elution test defined in "Test procedures for glass containers for injections" in "The Japanese Pharmacopoeia Fourteenth Edition; warming the solution at 70 ⁇ 5 °C for 1 hour, cooling the solution to the room temperature, removing the hollow fibers from the solution, and then adding distilled water to the solution to adjust its volume to 150 ml.
  • the absorbance is determined at the maximum absorption length within the range of 220 to 350 nm by ultraviolet absorption spectrum of the solution.
  • the criterion measure for absorbance is set to 0.1 or below.
  • Japanese patent laying-open No. JP2000-288085A discloses a method for preventing hollow fibers from being damaged by irradiation, which comprises the steps of controlling a water content of hollow fibers to ⁇ 5%, and a relative humidity of ambient atmosphere to ⁇ 40% when carrying out radiation sterilization.
  • Japanese patent laying-open No. JP2001-170167A discloses a method that comprises the steps of allowing hollow fibers to hold water accounting for 100 to 600% of the whole weight of the hollow fibers, and filling the blood-processing device with inert gas.
  • Japanese patent publication No. H5-50946 discloses a method comprising the steps of sealing a blood-processing device together with deoxidizer in a gas-impermeable container, and then subjecting the resultant sealed container to radiation sterilization.
  • the methods of the prior art have troubles in arrangements of radiation sterilization since they require strict control of the water content of the hollow fibers and relative humidity of the ambient atmosphere thereof, or processes of allowing hollow fibers to hold water and filling the interior of the blood-processing device with inert gas.
  • the hollow fiber blood-processing device is sealed together with the deoxidizer in the gas-impermeable container as disclosed in the above Patent document 3, the hollow fibers are damaged by irradiation, resulting in increase of extractables from the hollow fibers.
  • the hollow fibers are of polysulfone-based resin containing hydrophilic polymer, the extractables are considerably increased, resulting in failure to meet the above criterion measures.
  • WO98/58842 discloses a hollow fiber blood-processing device comprising a bundle of hollow fibers, sided together with a deoxidizer in a gas-impermeable container being radiation sterilised.
  • US 5,881,534A discloses a medical article of a polymeric material enclosed in a gas impermeable package together with an oxygen absorber and radiation sterilised.
  • the present invention has been made on the finding that oxygen deteriorates quality of hollow fibers, especially those of polysulfone-based resin and promotes damages of hollow fibers during radiation sterilization.
  • the material for the hollow fibers used in the blood processing device is a polysulfone-based resin containing a hydrophilic polymer.
  • Preferred polysulfone-based resin includes polysulfone and polyethersulfone.
  • a preferred hydrophilic polymer is polyvinylpyrrolidone.
  • the hollow fiber blood-processing device comprises a bundle of hollow fibers made of a polysulfone-based resin containing a hydrophilic polymer.
  • the interior of the blood-processing device and that of the container are in the oxygen free condition.
  • the sealed container holding the blood-processing device is left to stand for a time sufficient to allow the deoxidizer to absorb oxygen in the container after sealing of the container.
  • the blood-processing device of a hollow fiber type may be of a dry type.
  • the radiation sterilization may be gamma-radiation sterilization.
  • blood-processing device generally means a medical apparatus used for blood processing such as hemodialysis, hemofiltration, hemodiafiltration, plasma fraction and plasmapheresis.
  • the term "hollow fiber blood-processing device” means an apparatus of the kind wherein a plurality of yarns referred to as “hollow fibers” of various synthetic resins are bundled to form a hollow fiber bundle and wherein the hollow fiber bundle is housed in a cylindrical container.
  • the hollow fibers are required to have a property to selectively allow blood components to filter out, and to have an excellent biocompatibility including antithrombogenicity.
  • the materials for hollow fibers that comply with these requirements include natural cellulose, derivatives thereof such as cellulose diacetate, cellulose triacetate; high polymers prepared by copolymerization of a hydrophilic monomer and a hydrophobic monomer; and blends of hydrophilic polymer and polysulfone-based resin..
  • the hollow fiber blood-processing device comprises hollow fibers made of polysulfone-based resin containing hydrophilic polymer.
  • the polysulfone-based resin includes, for example, polysulfone and polyethersulfone.
  • the hydrophilic polymer is a polymer that is present in hollow fibers of polysulfone-based resin and provides the hollow fibers with hydrophilicity.
  • Such hydrophilic polymer includes, for example, polyvinylpyrrolidone (hereinafter referred to as "PVP") and polyethylene glycol.
  • PVP polyvinylpyrrolidone
  • preferred hydrophilic polymer is PVP in view of the efficacy of hydrophilicity and safety to use.
  • the hydrophilic polymer used in the present invention has a molecular weight of 10,000 to 1,200,000, preferably, 50,000 to 500,000.
  • a content of the hydrophilic polymers in the hollow fibers is 3 to 20 % by weight, preferably, 3 to 10 % by weight in respect to the total weight of the hollow fibers.
  • Examples of commercially available PVP are PVPK-15, 30, 60, 90(Trade name of ISP).
  • the hollow fibers may be manufactured by incorporating hydrophilic polymer into a concentrate solution for spinning, and then spinning yarns by dry or wet spinning.
  • the hollow fibers are manufactured by the steps of mixing polysulfone, hydrophilic polymer, a solvent thereof, an additive for controlling a pore size of micropores of the hollow fibers with stirring at an elevated temperature to prepare a homogeneous concentrate solution for spinning; extruding the resultant spinning solution comprises of polysulfone and hydrophilic polymer into a gas atmosphere through a ring portion of a double ring nozzle while expelling a lipophilic liquid such as liquid paraffin as a core liquid through a central portion of the nozzle, or feeding a gas such as nitrogen to form a hollow fiber as well as to form miropores in the hollow fibers.
  • the solvent used is a solvent that is able to dissolve both polysulfone-based resin and hydrophilic resin.
  • examples of usable solvents are N-methyl-2-pyrrolidone, dimethylsulfoxide and N-dimethylacetamide. These solvents may be used alone or in combination to adjust the solubility.
  • a preferred content of the solvent in the spinning solution ranges from 35 to 75 percent by weight.
  • the above solvent may be blended with a liquid as a nonsolvent that does not possess the solubility for both polysulfone-based resin and hydrophilic resin to adjust the solubility.
  • a nonsolvent include, for example, polyvalent alcohols such as monoethylene glycol, triethylene glycol, polyethylene glycol and glycerin; and lower alkylether derivatives of these polyvalent alcohols; which may be used alone or in combination with two or more materials.
  • the nonsolvent is preferably added to the spinning solution in the range of 7 to 35 percent by weight.
  • the additive for controlling pore size of the micropores includes, for example, liquid paraffin, isopropyl myristate, air, helium gas and nitrogen gas.
  • the gas atmosphere into which the spinning solution is extruded includes, without being limited to, air, nitrogen, oxygen, carbon dioxide, argon and helium. Generally, the atmosphere is air.
  • the hollow fibers used in the blood-processing device have an internal diameter ranging from 100 to 300 ⁇ m. If the internal diameter is less than 100 ⁇ m, it induces increase in pressure loss of the blood flowing through the hollow fibers, which gives rise to damages of the blood, causing a risk of destruction of red blood cells. Further, the internal diameter less than 100 ⁇ m may cause coagulation of the blood, causing a possibility of formation of a blood clot in the hollow portions. On the other hand, if the internal diameter exceeds 300 ⁇ m, hollow portions of the hollow fibers become too large to keep their hollow shape, resulting in decrease of productivity.
  • the hollow fibers have an inner diameter ranging from 120 to 250 ⁇ m.
  • the hollow fibers have a film thickness ranging from 10 to 50 ⁇ m. More preferred film thickness of the hollow fibers ranges from 10 to 30 ⁇ m.
  • the above hollow fibers may be modularized in a known manner, for example, by a method comprising the steps of bundling about 7000 to 12000 pieces of hollow fibers to form a hollow fiber bundle; inserting the resultant hollow fiber bundle into a cylindrical container; injecting a potting material into both ends of the container to seal each end of the container; cutting off the excess potting material together with the hollow fibers from each end of the container to open both ends of the hollow fibers, and mounting headers on each end of the container to complete a hollow fiber module.
  • materials for other components of the blood-processing device other than the hollow fibers e.g., the cylindrical container and potting material
  • materials for other components of the blood-processing device other than the hollow fibers e.g., the cylindrical container and potting material
  • Typical materials for the cylindrical container are exemplified by polycarbonate and polypropylene, but it is preferred to use polycarbonate that is excellent in both thermostability and transparency.
  • Typical materials for the potting material are exemplified by polyurethane, epoxy resin and silicone resin, but it is preferred to use polyurethane that is excellent in biocompatibility.
  • the deoxidizer or oxygen absorber is held in a sealed container together with the medical module, and thus the deoxidizer is required to be nontoxic.
  • the deoxidizer is a deoxidizer or an oxygen absorber of a water-releasing type that releases water at the time of absorption of oxygen.
  • the deoxidizer contains an active metal as a main component and has a controllable reaction rate with a catalyst.
  • active metals include, for example, iron, zinc, copper and tin. It is, however, preferred to use a deoxidizer comprising activated iron oxide in view of cost and deodorizing effects.
  • a gas-impermeable material for the sealed container holding the hollow fiber blood-processing device and the deoxidizer it is preferred to use a material with an oxygen-permeability of 1cm 3 /(m 2 ⁇ 24h ⁇ atm) or below, and a vapor-permeability of 5g/(m 2 ⁇ 24h ⁇ atm) or below.
  • Such a gas-impermeable material include, for example, oriented or unoriented films or sheets of polyvinylidene chloride, polyvinyl alcohol, polyamides and polyesters; films or sheets coated with these resins; laminated films or sheets of these films; laminated films or sheets of polyester/aluminum/polyethylene; four-layered, laminated films or sheets of polyethylene terephthalate/polyethylene/aluminum/polyethylene or nylon/polyethylene/aluminum/polyethylene; metal foils such as aluminum foil; deposited metal films such as deposited aluminum films, and laminated products of these films.
  • the preferred materials are four-layered, laminated films of polyethylene terephthalate/polyethylene/aluminum/poly-ethylene or nylon/polyethylene/aluminum/polyethylene.
  • the term "radiation sterilization” means a method for radiation sterilization of gamma rays or electron rays.
  • the radiation sterilization has various advantages: The sterilization can be applied to end products in which the product to be sterilized is held in a sealed container. Since the radiation sterilization can be carried out at the normal temperature, there is no fear of damages or degradation of the materials that may occur by the sterilization at elevated temperatures. Since there is no fear of formation of noxious residues such as noxious gases, the radiation sterilization is a safe method of sterilization. Further, it is easy to control the sterilization process, thus making it possible to continuously sterilize large quantities of products under the same conditions.
  • the irradiation of gamma rays may be carried out under the normally used conditions. It is sufficient for the sterilization to perform irradiation with 5 to 40 kGy, preferably, 10 to 20 kGy of gamma rays.
  • the hollow fiber blood-processing device generally divided into two types, i.e., an apparatus of the kind wherein a container that houses a hollow fiber bundle is filled with a liquid such as sterile water or distilled water (herein after referred to as a "wet type”), and an apparatus of the kind wherein a container that houses a hollow fiber bundle is not filled with a liquid (herein after referred to as a "dry type"). It is preferred to use a dry type. Because, the wet type has an increased weight and disadvantages for handling or transportation. In addition, there is a fear of freezing in winter seasons.
  • the wet type it is necessary for the wet type to prepare the liquid such as sterile water to be charged in the container, thus making it difficult to save the production cost of the blood-processing device.
  • the hollow fibers are held in the wet conditions that are easy for bacteria to bleed, there is a fear of bleeding of bacteria even in a short time before sterilization but after sealing.
  • the production of the wet type requires any refrigerating plant to prevent the hollow fibers from being bleeding of bacteria.
  • the dry type blood-processing device is free from the aforesaid problems since it contains no liquid in the container.
  • an interior of a cylindrical container i.e., a space holding the hollow fibers
  • the gas may be an atmospheric air that contains oxygen even at the time of sealing the gas impermeable container holding the blood-processing device.
  • the deoxidizer which absorbs oxygen in the sealed container is a water-releasing type deoxidizer.
  • the present invention it is possible to produce hollow fiber blood-processing devices with minimal extractables from the hollow fibers since the irradiation is carried out after holding the blood-processing device and the deoxidizer in the sealed container of the gas-impermeable material. Since the blood-processing device is kept in the oxygen free conditions before carrying out the radiation sterilization, it is possible to produce hollow fiber blood-processing devices with minimal extractables from the hollow fibers even if the hollow fibers are made of polysulfone-based resin containing hydrophilic polymer. In addition, the extractables from the hollow fibers are considerably reduced by use of the water-releasing type deoxidizer.
  • the present invention makes it possible to improve the shelf life of the blood-processing device even if the hollow fibers are of polysulfone-based resin that releases adsorbed oxygen during storage.
  • Fig. 1 is a cross section of a hollow fiber blood-processing device embodying the present invention.
  • a blood-processing device (1) of a hollow fiber membrane type which comprises a bundle (2) of a plurality of hollow fiber membranes, a cylindrical container (3) holding the hollow fiber bundle (2) therein.
  • the cylindrical body (3) has an inlet port (4) and an outlet port (5) each arranged in the proximity of each end of the cylindrical body (3).
  • Caps (6, 7) are mounted on each end of the cylindrical body (3) and provided with an inlet (8) and an outlet (9).
  • the hollow fiber membranes are made of, for example, polyethersulfone containing polyvinylpyrollidone, bundled together to form a hollow fiber bundle (2), inserted into the cylindrical body (3) and sealed at both ends thereof by a potting material 10.
  • the blood-processing device (1) is packaged in a gas-impermeable container (11) together with a deoxidizer (12) and then radiation sterilized in the following manner.
  • the hollow fiber blood-processing device (1) is put into the gas-impermeable container (11) together with the oxygen absorber (12) of a water-releasing type.
  • the gas-impermeable container is made of, for example, a four-layered laminated film of nylon/polyethylene/aluminum/polyethylene.
  • the container (11) is then sealed by thermal welding, and left to stand for a number of hours, preferably 12 hours or more, more preferably, 24 hours or more so that the interior of the container is made into an oxygen-free state. Then, the sealed container (11) is subjected to radiation sterilization to complete the sterilization.
  • hollow fiber blood-processing devices by bundling 9600 pieces of hollow fibers to form a hollow fiber bundle, inserting the hollow fiber bundle into a cylindrical container of polycarbonate, injecting a polyurethane potting material into both ends of the cylindrical container to seal the both ends thereof, cutting away some parts of the hollow fiber bundle from both ends thereof together with extra potting materials to allow the hollow fibers to be opened at both ends thereof, and mounting headers on both ends of the container to complete the hollow fiber blood-processing device of a dry type.
  • the blood-processing device is placed into a container made of a gas-impermeable material, i.e., a laminated film of polyester/aluminum/polyethylene together with an oxygen absorber, SANSOCUT (Trademark, Nittetsu Fine Products, Co. Ltd.). After sealing the container in the atmosphere, the container is left to stand for about 24 hours to allow the oxygen absorber to absorb oxygen in the sealed container to make the interior of the container into an oxygen-free state. The sealed container is then radiation sterilized by exposure to gamma rays of 15 kGy.
  • a gas-impermeable material i.e., a laminated film of polyester/aluminum/polyethylene together with an oxygen absorber, SANSOCUT (Trademark, Nittetsu Fine Products, Co. Ltd.).
  • Example 2 There were prepared hollow fiber blood-processing devices of a dry type in the same manner as in Example 1. Each device was put into a gas-impermeable container made of a laminated film of polyester/aluminum/polyethylene without use of any oxygen absorber. After sealing the container in the atmosphere, the sealed container is then radiation sterilized by exposure to gamma rays of 15 kGy.
  • Type of hollow fiber blood-processing device Dry type Material of hollow fibers: Polyethersulfone containing PVP Film thickness of hollow fibers 30 ⁇ m Internal diameter of hollow fibers 200 ⁇ m Gamma radiation 15 kGy Material for gas-impermeable container polyester/aluminum/polyethylene Time to radiation sterilization after sealing 24 hours
  • the absorbance of the test solution for extraction is 0.285, which does not meet the approval standards for artificial kidneys mentioned above.
  • the absorbance of the test solution for extraction is 0.055.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Emergency Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Vascular Medicine (AREA)
  • Anesthesiology (AREA)
  • Hematology (AREA)
  • External Artificial Organs (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Apparatus For Disinfection Or Sterilisation (AREA)
EP04255856A 2003-09-24 2004-09-24 Hollow fiber blood-processing device Expired - Lifetime EP1518564B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL04255856T PL1518564T3 (pl) 2003-09-24 2004-09-24 Urządzenie do obróbki krwi z wydrążonymi włóknami

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2003330974 2003-09-24
JP2003330973 2003-09-24
JP2003330973A JP4738728B2 (ja) 2003-09-24 2003-09-24 中空糸型血液処理器及びその滅菌包装方法
JP2003330974A JP4738729B2 (ja) 2003-09-24 2003-09-24 中空糸型血液処理器の滅菌包装方法

Publications (3)

Publication Number Publication Date
EP1518564A2 EP1518564A2 (en) 2005-03-30
EP1518564A3 EP1518564A3 (en) 2006-10-04
EP1518564B1 true EP1518564B1 (en) 2008-08-06

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EP04255856A Expired - Lifetime EP1518564B1 (en) 2003-09-24 2004-09-24 Hollow fiber blood-processing device

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US (1) US8211362B2 (es)
EP (1) EP1518564B1 (es)
CN (1) CN100563732C (es)
AT (1) ATE403446T1 (es)
AU (1) AU2004212619B2 (es)
CA (1) CA2481865C (es)
DE (1) DE602004015544D1 (es)
ES (1) ES2310703T3 (es)
PL (1) PL1518564T3 (es)
TW (1) TWI354571B (es)

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EP1795254B1 (en) * 2004-08-10 2014-05-21 Nipro Corporation Process for production of a polysulfone type selectively permeable hollow fiber membrane module
US20080000830A1 (en) * 2004-08-10 2008-01-03 Kimihiro Mabuchi Highly Water Permeable Hollow Fiber Membrane Type Blood Purifier and Process for Manufacturing the Same
JP4885437B2 (ja) * 2004-10-15 2012-02-29 東洋紡績株式会社 血液浄化器および血液浄化器包装体
JP4731875B2 (ja) 2004-10-15 2011-07-27 東洋紡績株式会社 血液浄化器の滅菌方法および血液浄化器包装体
US9067178B2 (en) * 2004-12-22 2015-06-30 Nipro Corporation Blood purifier package and process for manufacturing the same
JP3772909B1 (ja) * 2005-04-04 2006-05-10 東洋紡績株式会社 血液浄化器
KR100656294B1 (ko) * 2005-12-19 2006-12-11 연세대학교 산학협력단 중공사막 모듈과 중공사막 모듈 제조방법
MX2010003087A (es) 2007-09-21 2010-06-23 Enox Biopharma Inc Tubos para drenaje de oido con liberacion de gas antimicrobiano.
GB201300465D0 (en) 2013-01-11 2013-02-27 Aquaporin As A hollow fiber module having tfc-aquaporin modified membranes
DK177696B1 (en) 2013-02-25 2014-03-17 Aquaporin As Systems for water extraction
DE102014108530A1 (de) * 2014-06-17 2015-12-17 B. Braun Avitum Ag Verfahren zur Sterilisierung eines Hohlfaserfiltermoduls, Hohlfaserfiltermodul mit Verschluss und Sauerstoff absorbierender Verschluss
EP3202437B1 (en) * 2014-09-29 2018-11-21 Asahi Kasei Medical Co., Ltd. Hollow fiber membrane-type blood purification device
DE102016102087A1 (de) * 2016-02-05 2017-08-10 B. Braun Avitum Ag Filtermodul-Verpackungs-Einheit
DE102016102089A1 (de) * 2016-02-05 2017-08-10 B. Braun Avitum Ag Medizinische Sterilverpackungseinheit
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CA2481865C (en) 2011-07-05
PL1518564T3 (pl) 2009-01-30
AU2004212619A1 (en) 2005-04-07
AU2004212619B2 (en) 2009-12-17
US8211362B2 (en) 2012-07-03
ATE403446T1 (de) 2008-08-15
CA2481865A1 (en) 2005-03-24
DE602004015544D1 (de) 2008-09-18
EP1518564A3 (en) 2006-10-04
CN100563732C (zh) 2009-12-02
ES2310703T3 (es) 2009-01-16
TWI354571B (en) 2011-12-21
CN1600382A (zh) 2005-03-30
TW200514588A (en) 2005-05-01
US20050063859A1 (en) 2005-03-24
EP1518564A2 (en) 2005-03-30

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